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Topical calcineurin inhibitors, especially 0.1% tacrolimus ointment, are effective and well-tolerated for treating cutaneous lupus erythematosus but require more research for standard treatment guidelines.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Bicalutamide may be a promising alternative treatment for female pattern hair loss.

Combining hair transplantation with microneedling or laser and UV light may help treat tough vitiligo on hands and feet, with microneedling being affordable and easy to learn.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

The document concludes that proper treatment and management of plaque psoriasis in adolescents can improve their quality of life.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

New treatments for vitiligo may focus on protecting melanocyte stem cells from stress and targeting specific pathways involved in the condition.

The paper concludes that elderly in India face unique skin challenges and need better dermatological care and awareness.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

Early diagnosis and aggressive treatment are crucial for Cicatricial Alopecia, and treatment effectiveness varies among patients.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document concludes that better tools are needed to measure skin disease severity in dermatomyositis and cutaneous lupus erythematosus, and introduces the DSSI and CLASI as reliable instruments.

About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

Diagnosing new systemic lupus during pregnancy is hard but important for the health of the mother and baby.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Children's skin diseases and treatments differ from adults and require specific approaches.

Careful planning and accurate diagnosis are crucial for successful hair restoration surgery.

Spironolactone and clascoterone are promising acne treatments with fewer side effects.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

Different light affects cell functions and can help treat skin conditions.

Fever and rash can be early signs of lupus.

Recognizing unusual brain and skin symptoms is crucial for diagnosing lupus early.

Skin problems are common in lupus, often appearing first, with various types and treatments, and careful monitoring is important for diagnosis and management.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

Invasomes loaded with clotrimazole gel could improve drug delivery through the skin for fungal treatment.

It's unclear if COVID-19 vaccination causes SLE; more research is needed.